Myocardial Tissue Characterization in Heart Failure with Preserved Ejection Fraction: From Histopathology and Cardiac Magnetic Resonance Findings to Therapeutic Targets

被引:25
作者
Severino, Paolo [1 ]
D'Amato, Andrea [1 ]
Prosperi, Silvia [1 ]
Fanisio, Francesca [1 ]
Birtolo, Lucia Ilaria [1 ]
Costi, Bettina [1 ]
Netti, Lucrezia [1 ]
Chimenti, Cristina [1 ]
Lavalle, Carlo [1 ]
Maestrini, Viviana [1 ]
Mancone, Massimo [1 ]
Fedele, Francesco [1 ]
机构
[1] Sapienza Univ Rome, Dept Clin Internal Anesthesiol & Cardiovasc Sci, Viale Policlin 155, I-00161 Rome, Italy
关键词
heart failure; heart failure with preserved ejection fraction; myocardial tissue characterization; cardiac magnetic resonance; endomyocardial biopsy; therapy; CORONARY MICROVASCULAR DYSFUNCTION; VENTRICULAR DIASTOLIC FUNCTION; EXTRACELLULAR VOLUME FRACTION; EPICARDIAL ADIPOSE-TISSUE; OVERLOAD-INDUCED LEFT; ESC WORKING GROUP; EXERCISE CAPACITY; SYSTOLIC FUNCTION; CARDIOVASCULAR OUTCOMES; VASCULAR-PERMEABILITY;
D O I
10.3390/ijms22147650
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Heart failure with preserved ejection fraction (HFpEF) is a complex clinical syndrome responsible for high mortality and morbidity rates. It has an ever growing social and economic impact and a deeper knowledge of molecular and pathophysiological basis is essential for the ideal management of HFpEF patients. The association between HFpEF and traditional cardiovascular risk factors is known. However, myocardial alterations, as well as pathophysiological mechanisms involved are not completely defined. Under the definition of HFpEF there is a wide spectrum of different myocardial structural alterations. Myocardial hypertrophy and fibrosis, coronary microvascular dysfunction, oxidative stress and inflammation are only some of the main pathological detectable processes. Furthermore, there is a lack of effective pharmacological targets to improve HFpEF patients' outcomes and risk factors control is the primary and unique approach to treat those patients. Myocardial tissue characterization, through invasive and non-invasive techniques, such as endomyocardial biopsy and cardiac magnetic resonance respectively, may represent the starting point to understand the genetic, molecular and pathophysiological mechanisms underlying this complex syndrome. The correlation between histopathological findings and imaging aspects may be the future challenge for the earlier and large-scale HFpEF diagnosis, in order to plan a specific and effective treatment able to modify the disease's natural course.
引用
收藏
页数:28
相关论文
共 209 条
[41]  
Fedele F, 2013, FUTUR CARDIOL, V9, P897, DOI [10.2217/fca.13.65, 10.2217/FCA.13.65]
[42]   Role of genetic polymorphisms of ion channels in the pathophysiology of coronary microvascular dysfunction and ischemic heart disease [J].
Fedele, Francesco ;
Mancone, Massimo ;
Chilian, William M. ;
Severino, Paolo ;
Canali, Emanuele ;
Logan, Suzanna ;
De Marchis, Maria Laura ;
Volterrani, Maurizio ;
Palmirotta, Raffaele ;
Guadagni, Fiorella .
BASIC RESEARCH IN CARDIOLOGY, 2013, 108 (06)
[43]   miR-146a mediates inflammatory changes and fibrosis in the heart in diabetes [J].
Feng, Biao ;
Chen, Shali ;
Gordon, Andrew Devon ;
Chakrabarti, Subrata .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2017, 105 :70-76
[44]   Equilibrium Contrast Cardiovascular Magnetic Resonance for the Measurement of Diffuse Myocardial Fibrosis Preliminary Validation in Humans [J].
Flett, Andrew S. ;
Hayward, Martin P. ;
Ashworth, Michael T. ;
Hansen, Michael S. ;
Taylor, Andrew M. ;
Elliott, Perry M. ;
McGregor, Christopher ;
Moon, James C. .
CIRCULATION, 2010, 122 (02) :138-U72
[45]   Sex-specific microRNAs in women with diabetes and left ventricular diastolic dysfunction or HFpEF associate with microvascular injury [J].
Florijn, Barend W. ;
Valstar, Gideon B. ;
Duijs, Jacques M. G. J. ;
Menken, Roxana ;
Cramer, Maarten J. ;
Teske, Arco J. ;
Ghossein-Doha, Chahinda ;
Rutten, Frans H. ;
Spaanderman, Marc E. A. ;
den Ruijter, Hester M. ;
Bijkerk, Roel ;
van Zonneveld, Anton Jan .
SCIENTIFIC REPORTS, 2020, 10 (01)
[46]   Characteristics, treatments, and outcomes of patients with preserved systolic function hospitalized for heart failure - A report from the OPTIMIZE-HF registry [J].
Fonarow, Gregg C. ;
Stough, Wendy Gattis ;
Abraham, William T. ;
Albert, Nancy M. ;
Gheorghiade, Mihai ;
Greenberg, Barry H. ;
O'Connor, Christopher M. ;
Sun, Jie Lena ;
Yancy, Clyde W. ;
Young, James B. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2007, 50 (08) :768-777
[47]   LEFT-VENTRICULAR DIASTOLIC FUNCTION IN HYPERTENSION - RELATION TO LEFT-VENTRICULAR MASS AND SYSTOLIC FUNCTION [J].
FOUAD, FM ;
SLOMINSKI, JM ;
TARAZI, RC .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1984, 3 (06) :1500-1506
[48]   Quantification of diffuse myocardial fibrosis using CMR extracellular volume fraction and serum biomarkers of collagen turnover with histologic quantification as standard of reference [J].
Foussier, C. ;
Barral, P. A. ;
Jerosh-Herold, M. ;
Gariboldi, V. ;
Rapacchi, S. ;
Gallon, A. ;
Bartoli, A. ;
Bentatou, Z. ;
Guye, M. ;
Bernard, M. ;
Jacquier, A. .
DIAGNOSTIC AND INTERVENTIONAL IMAGING, 2021, 102 (03) :163-169
[49]   The role of titin and extracellular matrix remodelling in heart failure with preserved ejection fraction [J].
Franssen, C. ;
Gonzalez Miqueo, A. .
NETHERLANDS HEART JOURNAL, 2016, 24 (04) :259-267
[50]   Probing SGLT2 as a therapeutic target for diabetes: Basic physiology and consequences [J].
Gallo, Linda A. ;
Wright, Ernest M. ;
Vallon, Volker .
DIABETES & VASCULAR DISEASE RESEARCH, 2015, 12 (02) :78-89